| HS Code | 222538 |
| Productname | LyondellBasell Starflex mLLDPE GM1810BB |
| Polymertype | Metallocene Linear Low Density Polyethylene (mLLDPE) |
| Comonomer | Butene |
| Physicalform | Pellets |
| Density | 0.918 g/cm³ |
| Meltindex 190c 2 16kg | 1.0 g/10 min |
| Meltingpoint | 116 °C |
| Vicatsofteningpoint | 94 °C |
| Tensilestrengthatyield | 10 MPa |
| Tensilestrengthatbreak | 25 MPa |
| Elongationatbreak | 600% |
| Flexuralmodulus | 240 MPa |
| Dartdropimpact | 1200 g |
| Haze | 5% |
| Gloss45 | 85 |
| Sealinitiationtemperature | 95 °C |
As an accredited LyondellBasell Starflex mLLDPE GM1810BB factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | LyondellBasell Starflex mLLDPE GM1810BB is typically supplied in sealed 25 kg bags, 55 bags per 1,375 kg pallet. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with palletized bags of LyondellBasell Starflex mLLDPE GM1810BB, properly stowed, secured, and sealed for export. |
| Shipping | LyondellBasell Starflex mLLDPE GM1810BB is shipped as non-hazardous polyethylene pellets in sealed bags or octabins. Keep dry and protect from heat, moisture, and contamination; transport under ambient conditions. It is typically not regulated as dangerous goods, but follow local packaging, labeling, and handling regulations. |
| Storage | Store LyondellBasell Starflex mLLDPE GM1810BB in a cool, dry, well-ventilated area, away from direct sunlight, heat, moisture, and ignition sources. Keep original bags or containers closed, clean, and palletized to prevent contamination and dust accumulation. Avoid prolonged UV exposure, excessive stacking, and high temperatures. Follow the manufacturer’s SDS and local regulations for safe handling and storage. |
| Shelf Life | Typically 24 months from production when stored in original, unopened packaging under dry conditions, away from direct sunlight and heat. |
Coextruded cast film structures for high-speed vertical form-fill-seal (VFFS) packaging lines often position LyondellBasell Starflex mLLDPE GM1810BB in the sealant layer at 15–20 μm within a 45–70 μm overall film, with the core or skin layer composed of propylene-ethylene random copolymer or medium-density polyethylene. The metallocene molecular architecture narrows the melting distribution, permitting sealing jaw setpoints of 95–110 °C when seal dwell time is 20–40 ms and pressure is 2.0–4.0 N/cm². Hot tack is evaluated on a J&B Hot Tack Tester with a seal dwell time of 100 ms and a cooling time of 100 ms; target hot tack strength at 110 °C is 2.0–3.5 N/15 mm under ASTM F1921/F1921M-12(2023). On a production-scale cast film line with 90 mm screw diameter and 30:1 L/D, melt temperature is normally maintained at 240–260 °C, and chill roll temperature is held at 18–25 °C. If chill roll temperature exceeds 28 °C, film surface roughness increases and transfer roll wrap may destabilize web tension. Blending GM1810BB with 20–30 wt% LDPE having melt flow rate of 4.0 g/10 min reduces neck-in and edge bead while maintaining hot tack. Final pouches for frozen vegetables, dry snacks, and shredded cheese are produced on VFFS lines cycling at 50–70 packs/min. Food contact compliance under EU 10/2011 requires overall migration below 10 mg/dm² when tested under EN 1186-1; for fatty foods, simulant D2 or 95% ethanol is applied. In the United States, FDA 21 CFR 177.1520 covers olefin polymers, and extraction testing follows 21 CFR 177.1520(d). Pre-drying is normally not required below 60% relative humidity. At higher ambient humidity, surface moisture on pellets can increase melt pressure fluctuation in the extruder and should be addressed with hopper drying at 70–80 °C for 2–4 h.
For adhesive-laminated pouches used in frozen food, reverse-printed BOPET or BOPP outer webs are bonded to a GM1810BB sealant web at 40–60 μm, bonded by a two-component polyurethane adhesive applied at 2.0–3.5 g/m² dry coat weight. The sealant film is corona-treated to 42–46 dyn/cm before lamination; lower dyne levels produce uneven adhesive wet-out and risk delamination at the sealant-adhesive interface. The low seal initiation temperature of metallocene LLDPE permits heat seal settings at 105–125 °C on rotary pouch lines, but the sealing layer must be formulated with slip packages that do not bloom excessively during 24–48 h adhesive curing at 35–45 °C. High erucamide levels above 1,000 ppm can migrate to the treated surface and reduce bond strength below 1.5 N/15 mm when tested according to ASTM F88/F88M-21. Interlayer adhesion is also influenced by the choice of adhesive hardener: aromatic isocyanates may require longer curing times, while aliphatic hardeners reduce yellowing but increase cost. Finished pouches are filled on horizontal form-fill-seal lines at 40–60 packs/min, with burst strength tested under ASTM F2054-21 at internal pressure above 35 kPa for liquid products. Operational boundaries include limiting storage of treated film to 30 days at 20 °C and 50% RH because corona treatment decays with time and re-treatment may be required.
Blown film extrusion of GM1810BB for fresh produce bags requires a die gap of 1.5–2.2 mm, a blow-up ratio of 1.8:1–2.2:1, and a dual-lip air ring with chilled air at 8–12 °C to stabilize the bubble. The melt temperature is normally held at 190–220 °C, lower than conventional LLDPE to reduce oxidative degradation. Because metallocene LLDPE has lower shear sensitivity, extruder head pressure on a 75 mm grooved-feed extruder with 25:1 L/D can be 35–45 MPa depending on die diameter and throughput. High-clarity produce bags use 80–100 wt% GM1810BB with a small amount of LDPE for bubble stability, yielding haze values of 4–7% at 25 μm thickness when measured under ASTM D1003-21. Dart impact resistance at this thickness is typically above 150 g under ASTM D1709-22, and Elmendorf tear strength is higher in the machine direction at 100–150 g under ASTM D1922-15(2020), while transverse tear can be lower due to orientation effects. Perforation patterns are applied in-line by needle rollers for ventilation. Bags for leafy greens, citrus, and root vegetables are produced at 80–120 bags/min with fold-seal or side-seal configurations. Compliance with EU 10/2011 is required for direct food contact; specific migration of primary aromatic amines is not applicable because no polyurethane components are present. The main processing risk is bubble instability at high frost line height; if the frost line is set too high, melt strength decreases and the bubble sways, causing gauge variation of ±8% or more. Adding 5–15 wt% LDPE with melt flow rate of 0.25 g/10 min increases melt tension but raises haze.
When GM1810BB replaces conventional LDPE in heavy-duty sack inner liners at 20–40 wt% within a HDPE or medium-density polyethylene matrix, the coextruded blown film achieves a balance of low-temperature puncture resistance and contamination-free sealing for fertilizers, polymer pellets, and mineral powders. The film is produced on a three-layer blown film line with die gap 2.0–2.5 mm, blow-up ratio 1.6:1–2.0:1, and melt temperature 200–230 °C; the inner liner layer uses GM1810BB at 30 wt% while the outer layers use HDPE for stiffness. The finished liner thickness is 80–120 μm, and dart impact is tested under ASTM D1709-22 at method A or B depending on film thickness, with typical values exceeding 400 g for 100 μm film. Tensile properties are measured under ISO 527-3:2018, with machine direction elongation at break above 600%. Environmental stress crack resistance of the HDPE-rich layers is evaluated under ASTM D1693-21 in 10% Igepal CO-630 at 50 °C; GM1810BB contributes seal integrity without the higher extractables seen with some conventional low-density grades. The main processing constraint is screw recovery time: because GM1810BB has a melt flow rate of 1.0 g/10 min, higher back pressure may extend cycle time on smaller extruders below 75 mm. Additive packages for chemical powder liners often exclude oleamide and erucamide when the liner contacts fine powders that can adhere to the surface; instead, silica anti-block is used at 2,000–4,000 ppm. Pre-drying is required only if pellet surface moisture exceeds 500 ppm.
In hygiene backsheet extrusion for diaper and adult incontinence products, GM1810BB serves as the polyolefin carrier in calcium carbonate-filled breathable compounds at 45–55 wt% CaCO₃ with stearic acid surface treatment. Cast film lines with 100 mm screw and 33:1 L/D process the compound at 230–250 °C to ensure homogeneous dispersion; film thickness before stretching is 30–40 μm, and after machine-direction orientation at 2.5:1–3.5:1 stretch ratio, the film becomes microporous with air permeability measured as gurley values between 1,500–4,000 s/100 mL under ISO 5636-5:2013. The metallocene LLDPE carrier provides higher elongation before break and more uniform film thickness than conventional LLDPE, but melt pressure can rise above 30 MPa if calcium carbonate particle size is below 2 μm due to increased particle surface area. The breathable sheet is subsequently laminated to a polypropylene spunbond nonwoven with hot-melt adhesive at 1.5–3.0 g/m² to prevent fiber strike-through. The final backsheet must meet European REACH restrictions for substances of very high concern; U.S. FDA contact is not normally required for backsheet applications unless adhesion to the top sheet is direct. Processing limitations include screw torque constraints: a 100 mm extruder with 500 kW drive may operate near 80–90% torque, and screen pack changes are required every 4–6 h if calcium carbonate dispersion is poor.
Collation shrink film for bottling lines is extruded as a biaxially oriented shrink film using a blown film line with high-stalk bubble configuration and in-line orientation. GM1810BB is incorporated at 10–20 wt% into an LDPE/EVA base. The film is produced at thickness 45–60 μm, with blow-up ratio 2.0:1–2.5:1 and frost line height 20–25 cm above the die. Shrinkage is measured after 10 s immersion in an oil bath at 110 °C under ISO 14616:2017; typical transverse direction shrinkage is 15–20%, while machine direction shrinkage is 5–10%. Increasing GM1810BB content beyond 20 wt% can reduce shrinkage forces because the metallocene resin has lower crystallinity and lower orientation retention. Seal performance of shrink film on high-speed multipack lines requires seal initiation below 120 °C to avoid film relaxation before the shrink tunnel. The final film wraps PET bottles in 2×3, 4×3, or 2×2 configurations at speeds of 60–80 packs/min. A critical operational boundary is the shrink tunnel temperature: above 180 °C, the film can wrinkle and shrink force becomes non-uniform.
For aluminium foil extrusion lamination used in moisture-sensitive chemical packaging, GM1810BB is applied as a melt curtain at 25–35 μm thickness between aluminium foil and a low-density polyethylene sealant layer or directly onto kraft paper. The extruder is typically a 90 mm single-screw machine with 30:1 L/D and a T-slot die; melt temperature at the die is 280–300 °C to achieve oxidative adhesion, and the air gap is set at 80–120 mm to control neck-in. Corrosion-resistant tooling is required because molten polyethylene can generate acetic acid traces from oxidative degradation at high temperature. Laminated web adhesion is measured under ASTM D903-98(2017) or ASTM F904-16 and should exceed 1.0 N/15 mm for foil-to-film lamination. Final packages include foil-lined bags for hygroscopic chemical powders, desiccant pouches, and barrier sachets for oxygen-sensitive catalysts. The main incompatibility is excessive slip additive at the foil interface; erucamide levels above 800 ppm can reduce adhesion. Preheating of foil at 40–60 °C improves wet-out and lowers the required melt temperature. Published data for this specific configuration is limited, so line trials are recommended to set oxidative level.
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Polymers intended for high-speed cast stretch-film coextrusion are specified less by nominal density alone than by the combination of melt rheology, gel load, and additive-package consistency. LyondellBasell Starflex mLLDPE GM1810BB is a metallocene-catalysed linear low-density polyethylene identified within the Starflex range for cast film applications where downgauging, pallet-wrap holding force, and consistent unwind behaviour are primary converter requirements. The grade designation consists of the GM1810 base resin and a BB additive formulation; exact additive disclosure is controlled by the supplier safety data sheet and certificate of analysis rather than by the commercial grade name.
Two lot-release parameters dominate incoming resin control for this product. Density, measured by ISO 1183-1:2019 at 23 °C, is typically 0.918 g/cm³. Melt mass-flow rate, measured by ISO 1133-1:2022 at 190 °C and 2.16 kg, is typically 1.0 g/10 min. The combination of 0.918 g/cm³ density and 1.0 g/10 min melt flow rate places GM1810BB in a rheological region that favours melt strength during draw-down, but raises torque demand relative to 2.0 g/10 min or higher mLLDPE grades commonly used for very low-gauge hand-wrap films. Converters should not infer lot-specific compliance from these typical values; the certificate of analysis remains the governing document for each silo delivery.
Metallocene catalysis produces a narrower molecular weight distribution and a more homogeneous intermolecular comonomer distribution than conventional Ziegler-Natta catalysts operating in a gas-phase or slurry loop. High-temperature GPC under ISO 16014-1:2019 typically shows a lower dispersity for a metallocene ethylene-alpha-olefin copolymer than for a Ziegler-Natta butene-1 LLDPE of matching 0.918 g/cm³ density. The resulting film structure reduces the concentration of large, poorly solvated high-molecular-weight fractions that otherwise contribute to gel-like optical defects in 12–25 µm cast film. Compared with butene-1 LLDPE, the higher alpha-olefin comonomer type associated with many Starflex mLLDPE grades can shift the dart-impact–tear balance; however, published data for the specific comonomer of GM1810BB is limited in public literature, and converter-side film testing under ASTM D1709 and ASTM D1922 should be used for final specification.
On a 90 mm grooved-feed single-screw extruder with 30:1 L/D and a barrier-type screw, the lower melt index of GM1810BB increases specific energy consumption relative to 2.0 g/10 min grades. Plant logs from cast lines running 500–800 m/min often show that melt pressure at the screen changer rises for mLLDPE with narrow molecular weight distribution, and the use of a 60/100/60 mesh screen pack may require a reduction in throughput if the melt temperature exceeds 250 °C. Specific mechanical energy consumption on a 75 mm extruder is commonly recorded in the range of 0.18–0.25 kWh/kg for this melt-flow region, with the higher edge occurring when screen packs load with gel and oxidised material. This behaviour is not a resin defect; it is the physical consequence of a lower melt-flow rate and a more uniform molecular architecture.
Sharkskin and cyclic melt fracture are controlled by the shear stress at the die lip, not by melt flow rate alone. In flat-die cast film processes with a lip gap of 0.5–0.8 mm, surface defects may appear when the apparent die-lip shear stress moves above 0.1–0.2 MPa for a low-melt-index mLLDPE at 230–250 °C melt temperature. The addition of fluoropolymer processing aid, typically at 200–500 ppm, shifts defect onset to higher output by coating die metal surfaces. For GM1810BB, a die gap of 0.7–1.0 mm is commonly maintained on multilayer cast lines to handle both melt pressure and gauge uniformity; the exact optimum depends on die width, backpressure, and the presence of a coextrusion feedback loop. Below 210 °C melt temperature, surface melt fracture risk increases sharply, while excursions above 260 °C may increase carbonyl index and off-odour from thermal degradation of the additive package. On some lines the effective processing window is therefore held within ±5 °C of 240 °C to keep melt pressure and die-lip shear within stable limits.
Ambient pellet handling requires no pre-drying for polyethylene with a moisture content below 0.01 %. If resin has been stored in an unheated warehouse below dew point, surface condensation on pellets can produce feed-throat slip and minor film streaking; a 2–4 h tempering period inside a climate-controlled mezzanine is sufficient to remove surface water. Resin that has been exposed to dust from recycling processes should be passed through a magnetic grid and a 250 µm fine-mesh screen to protect the extruder screw and die lips. Avoid extended hold-up in stagnant melt zones because the metallocene resin can degrade locally and generate black specks or surface roughness that are not visible in incoming pellet inspection.
Because GM1810BB has a melt flow rate of 1.0 g/10 min, the available processing window is narrower than for higher-flow grades in the Starflex range. For a 75 mm 30:1 L/D extruder delivering 250–350 kg/h, barrel zone settings from feed to metering typically begin at 180 °C and rise to 230–245 °C, depending on screw design. Higher metering temperatures reduce melt viscosity and die-lip shear stress but increase the risk of odour, gel formation from degraded additive, and thermal degradation if residence time exceeds 5–8 min. Draw resonance in the air gap is a further constraint: for a low-melt-index mLLDPE, critical draw ratio is often observed between 20:1 and 30:1 at an air gap of 50–100 mm. Narrower air gaps tend to reduce the critical draw ratio, while higher melt temperatures increase it. The lower flow grade should be started up at reduced screw speed and gradual temperature soak to avoid high cold-start torque that can trip variable-frequency drive overloads.
Film haze, gloss, and coefficient of friction are not fixed by resin density alone; they are controlled by the BB additive package and by downstream cooling conditions. Haze testing under ASTM D1003 on 25 µm cast film should be performed after 24 h conditioning at 23 °C and 50 % relative humidity because antiblock migration and surface morphology change with time. Gloss at 45° under ASTM D2457 is strongly affected by chill-roll temperature and surface replication. Published data for the specific BB formulation are limited; converter-side trials should therefore quantify static and kinetic coefficient of friction according to ISO 8295:2004 on film wound at production tension, rather than extrapolating from resin-only data. If cling-layer additives from coextruded surfaces are present, the measured coefficient of friction can drift for more than 48 h after winding because migration kinetics in the polymer matrix are rate-limited and temperature-dependent.
In A/B/C cast stretch-film construction, GM1810BB is often considered for core and non-cling outer layers where machine-direction tear resistance and puncture propagation energy are critical. The cling layer typically uses a lower-density ethylene-vinyl acetate or specialty polyisobutylene-modified resin, which introduces a different migration dynamic. Because slip agents from the BB formulation can migrate to the cling-layer interface, the final unwind force at 200 % stretch is a system property, not a neat resin property, and must be tested on a stretch-film test stand under ISO 527-3 tensile conditions after the film has been stored for at least 48 h. Puncture propagation energy measured by ASTM D5748 on 12 µm film is similarly dependent on cling-layer composition and stretch history, not solely on the GM1810BB core layer.
Polyethylene converters often assume that resin food-contact status transfers automatically to the finished film. This assumption is incorrect under EU No 10/2011 and FDA 21 CFR 177.1520. The supplier may list the base olefin polymer and additives as permitted, but the final article must be tested for overall migration and specific migration limits under the intended temperature and food-simulant conditions. The BB additive package is not specified by the grade name alone; the safety data sheet and food-contact statement must be obtained from LyondellBasell for the exact lot. The table below identifies the standards that converters most often reference in raw-material certification.
| Regulatory framework | Standard or designation | Converter requirement |
|---|---|---|
| European Union food contact | EU No 10/2011 | Finished-article migration testing under intended simulant and time–temperature conditions |
| United States food contact | FDA 21 CFR 177.1520(c) | Verify olefin polymer specification and additive status in the final formulation |
| Chemical registration | REACH (EC) No 1907/2006 | Confirm monomer and additive registration status via extended SDS |
| Hazardous substances in electrical equipment | RoHS 2011/65/EU | Not normally applicable to polyethylene stretch film; confirm no recycled contamination |
| Film mechanical testing | ASTM D882, ISO 527-3 | Establish directional tensile properties on film of target gauge, not injection-moulded plaques |
Compared with a higher-flow Starflex grade used in hand-wrap stretch film, GM1810BB will generally require a larger die gap or a higher melt temperature to maintain equivalent throughput. Compared with an autoclave low-density polyethylene, it lacks the high-molecular-weight long-chain branching that stabilises blown-film bubbles at low melt temperatures; therefore it is not a drop-in replacement for LDPE in high-bubble-stability tubular film processes without blending. Blending with 10–20 % LDPE can improve neck-in control and bubble stability, but it also changes haze and tear performance, so blend ratios should be locked after ASTM D1922 tear testing on production film. These are operational boundaries derived from standard film-converting practice.